Successful treatment of histiocytic sarcoma with cladribine and high-dose cytosine arabinoside in a child

Haruko Iwabuchi, Hiroyuki Kawashima, Hajime Umezu, Takayuki Takachi, Masaru Imamura, Akihiko Saitoh, Akira Ogose, Chihaya Imai*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

Histiocytic sarcoma, a rare hematopoietic neoplasm with evidence of histiocytic differentiation, is often refractory to conventional chemotherapy and radiotherapy, and its prognosis is generally dismal. The optimal management of this malignancy has not been established. We report a case of 8-year-old girl with histiocytic sarcoma involving the left femur. The tumor rapidly responded to a combination of cladribine and high-dose cytosine arabinoside, an aggressive salvage regimen for refractory Langerhans cell histiocytosis, and became impalpable during the first cycle. The patient has remained in complete remission more than 7 years from diagnosis.

Original languageEnglish
Pages (from-to)299-303
Number of pages5
JournalInternational Journal of Hematology
Volume106
Issue number2
DOIs
StatePublished - 2017/08/01

Keywords

  • Cladribine
  • Cytosine arabinoside
  • Histiocytic sarcoma

ASJC Scopus subject areas

  • Hematology

Fingerprint

Dive into the research topics of 'Successful treatment of histiocytic sarcoma with cladribine and high-dose cytosine arabinoside in a child'. Together they form a unique fingerprint.

Cite this